QA Specialist, Supplier Quality
RoslinCT
Who We Are RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science. Who We Are RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science. THE ROSLINCT WAY Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients. ACCELERATING YOUR FUTURE The Quality Assurance Specialist – Supplier Quality supports quality activities related to Supplier Quality Management in compliance with FDA regulations and internal SOP’s. Responsibilities include supplier documentation management, change management, performance monitoring, leading supplier-related corrective actions and investigations, and audit support. How You Will Make an Impact: Provide support the supplier qualification program by: Onboarding new suppliers in support of new client programs Maintenance of supplier qualification documentation including questionnaires and quality agreements Support scheduling of audits and maintenance of the vendor audit schedule Support supplier audits and review of supplier response documentation Collaborate internally with key stakeholders in Supply Chain, Purchasing/Procurement, and Manufacturing Manage the Supplier Change Notification Program Review change notifications with cross-functional team and accelerate customer and supplier notifications with potential impact Support change controls for raw material or supplier-related updates Monitor Supplier Corrective Action Request (SCAR) Program Maintain SCAR Log and initiate supplier corrective action activities resulting from deviations, non-conforming material reports, and/or supplier audits Follow up on action items to ensure completion What You Will Bring: A highly organized work style that ensures timely execution of tasks. A mindset that ensures accurate results. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint). Effective problem-solving capabilities. Strong oral and written communication skills. Qualifications: B.S., in science, engineering, biochemistry, or related discipline, or combination of education, experience and training. Experience in cell therapy is a plus. 3+ years with directly relevant experience in a regulated environment, biopharmaceutical environment or similar. Working knowledge of supplier quality, including supplier assessments/audits, maintaining supplier evaluation program, supplier corrective actions, and supplier process changes. Practical knowledge of US and EU cGMP regulations and guidance, GMP and GLP regulations. Past experience of participation in or leading internal or supplier audits Strong communication skills (written and verbal), influencing, negotiating and collaboration skills. Demonstrate strong organizational skills including ability to prioritize tasks and adhere to agreed timelines. Ability to manage and deliver multiple tasks with limited supervision. Travel may be required up to 10% of the time. OUR COMMITMENT All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. RoslinCT is proud to be an equal-opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics. #J-18808-Ljbffr RoslinCT
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$38 - $40 per hour
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A leading medical device firm in Hudson, MA is seeking a Sr. Director, Design and Supplier Quality Assurance. This role involves global leadership for NPI design controls and ensuring compliance with quality standards. Candidates must possess a Bachelor's degree in engineering...Quality- ...medical device industry? At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of... ...environment and have a strong background in regulatory compliance and quality assurance, this is your opportunity to make a meaningful...Quality
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$24 - $29 per hour
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- Replimune is seeking a Senior Associate, Plant Quality Assurance to provide day‑to‑day quality oversight for drug substance, drug product, and quality control operations in support of cGMP and GDP. This on‑site role in Framingham collaborates with Manufacturing and Quality...Quality
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$99.5k - $128.5k
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$29.81 - $32.21 per hour
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